Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 976934생성일: 2026년 10월 24일
Ammonium Sulfate → 4-Amino-2-phenyl-8-[2-deoxy-3,5-di-O-(4-chlorobenzoyl)-beta-D-ribofuranosyl]-pteridine-7-one
https://huagongshe.com/ko/reaction/976934
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Ammonium Sulfate | HCID 6097028 | — |
| 반응물 | alpha-D-erythro-Pentofuranosyl chloride, 2-deoxy-, 3,5-bis(4-chlorobenzoate) | HCID 9845541 | — |
| 반응물 | 4-Amino-2-phenyl-pteridine-7-one | HCID 54402511 | — |
| 촉매 | Silver perchlorate | HCID 24562 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Hexamethyldisilazane | HCID 13838 | — |
| 생성물 | 4-Amino-2-phenyl-8-[2-deoxy-3,5-di-O-(4-chlorobenzoyl)-beta-D-ribofuranosyl]-pteridine-7-one | HCID 15403909 | — |
반응 단계
A mixture of 1.0 g (4.2 mmol) of 4-amino-2-phenyl-pteridine-7-one (3) and a few crystals of ammonium sulfate was heated in 100 mL of hexamethyldisilazane (HMDS) under reflux for 4 hours. After cooling the excess HMDS was distilled off in vacuum and the residue dissolved in 100 mL of dry toluene. To the mixture was added 2.17 g (4.6 mmol) of 2-deoxy-3,5-di-O-(4-chlorobenzoyl)-α-D-ribofuranosyl chloride (made as in Example 3, step (a) for the toluyl derivative) and 0.476 g (2.3 mmol) of silver perchlorate. The solution was then stirred under anhydrous conditions for 24 hours at room temperature and then diluted with 200 mL of CH2Cl2. The resulting AgCl precipitate was filtered off through silica and then the filtrate was treated with 100 mL of a saturated aqueous solution of sodium bicarbonate followed by 100 mL of a saturated aqueous solution of NaCl. The organic layer was dried over Na2SO4, filtered and then the filtrate evaporated.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05612468 |
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| 출처 데이터셋 | uspto-grants-1997_03 |
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| ORD ID | ord-e1b73d28aa304de09ead78bae0f1502b |
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| 출처 메모 | uspto-grants-1997_03 |
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